Submitted by Celso Magalhaes (celsomagalhaes@ufrrj.br) on 2018-08-30T16:36:02Z No. of bitstreams: 1 2009 - Aldir Carlos Silva.pdf: 1230710 bytes, checksum: 56dbab398ff37045b73bd259ab1a15ac (MD5) / Made available in DSpace on 2018-08-30T16:36:02Z (GMT). No. of bitstreams: 1 2009 - Aldir Carlos Silva.pdf: 1230710 bytes, checksum: 56dbab398ff37045b73bd259ab1a15ac (MD5) Previous issue date: 2009-03-06 / Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico - CNPq / Aluminum tolerance studies in seedlings of Passion fruit (cvs. IAC-273/277, IACPaulista, IAC-275, FB-100) and Carica papaya (cvs.Taiung, Golden, Gran Golden, Baixinho de Santa Amalia) were performed in a growth chamber at the Laboratories of Chemistry of the Rhizosphere and Seeds of the Department of Fitotecnia, of University Federal Rural of Rio Janeiro, Institute of Agronomy. Experiments with different concentrations of Al were conducted in nutrient solution simple (with Ca) and complete, with the aims to analyze the tap root length, ratio of root lengths, relative root elongation, diameter of root and stem and effect of stains. Also were conducted experiments with seeds soaked in different concentration of Al to verify the percentage of germination, seedlings normal and abnormal. The use of simple nutrient solution was not satisfactory to shown the performance of seedlings of papaya. In passion fruit both nutrient solutions can be used in short term experiment. Over the concentration of 160?M of Al occurred effect of toxicity in root of seedlings of passion fruit and papaya, but at concentrations lower that 80?M there were stimulus of growth. The tap root length was the more efficient parameter to compare root toxicity. The soaking of seeds in the solution of aluminum did not affect the germination, root tap emission and the growth of seedlings until 1280?M. With the increased of time of contact with the Al solution, the young roots have been injured especially in papaya seedlings. The use of stains pyrocatechol violet and hematoxylin were both efficient to determinate the aluminum tolerance in papaya and passion fruit, but just pyrocatechol violet could compare the doses used, produced a color gradient with increasing concentration of aluminum. With the use of hematoxylin was only possible to separate the high concentrations of low concentrations of aluminum. The best passion fruit cultivar was IAC 273/277and papaya was Tainung / Os estudos da toler?ncia ao alum?nio em pl?ntulas de maracuj? (cvs. IAC-273/277, IACPaulista, IAC-275, FB-100) e mam?o (cvs.Tainug, Golden, Gran Golden, Baixinho de Santa Am?lia) foram realizados, em c?mara de crescimento nos Laborat?rios de Qu?mica da Rizosfera e Laborat?rio de Analise de Sementes, Departamento de Fitotecnia, Instituto de Agronomia da Universidade Federal Rural Rio de Janeiro. Foram realizados experimentos com diferentes concentra??es de alum?nio em solu??o nutritiva simples (com c?lcio) e completa, para analise do crescimento radicular utilizando os par?metros comprimento radicular, taxa de crescimento radicular, elonga??o radicular relativa, di?metro do colo, di?metro de ?pice da raiz principal bem como testes com corantes. Foi tamb?m realizado estudos do efeito da embebi??o das sementes com solu??es de alum?nio para verificar o efeito na porcentagem de germina??o, pl?ntulas normais e anormais, e n?o germinadas. O uso da solu??o nutritiva simples para realizar testes de curta dura??o de contacto ao alum?nio, n?o foi satisfat?rio para mam?o, sendo mais adequado o uso de solu??o nutritiva completa. Em maracuj?, ambas as solu??es podem ser utilizadas. As pl?ntulas de maracuj? crescidas em solu??o simples com o aumento do tempo de contacto com alum?nio na solu??o, as ra?zes ficaram endurecidas. Em concentra??es acima de 160?M de alum?nio, ocorreu efeito fitotoxico, contudo em concentra??es menores que 80?M ocorreu at? aumento do crescimento radicular para mam?o e maracuj?. O comprimento radicular foi o mais eficiente par?metro indicador da toler?ncia ao alum?nio. A embebi??o das sementes em alum?nio n?o afetou a germina??o a emiss?o da raiz principal e o crescimento da pl?ntula at? a concentra??o da solu??o de embebi??o de 1280?M, mas a medida que aumentou o tempo de contato e a concentra??o de alum?nio, as ra?zes rec?m emitidas sofreram danos, principalmente as de pl?ntulas de mam?o. O uso dos corantes qu?micos violeta de pirocatecol e hematoxilina foram eficiente na determina??o da toler?ncia ao alum?nio em maracuj? e mam?o, mais somente o violeta de pirocatecol permitiu comparar as doses entre si, gerando um gradiente de colora??o com o aumento da concentra??o de alum?nio, com o uso da hematoxilina s? foi poss?vel separar as concentra??es altas das concentra??es baixas de alum?nio. As melhores cultivares nas condi??es testadas foi a IAC 273/277 de maracuj? e a cv Tainung de mam?o

Submitted by Sandra Pereira (srpereira@ufrrj.br) on 2017-05-12T14:19:07Z No. of bitstreams: 1 2010 - Henriqueta Talita Guimar?es Barboza.pdf: 10302674 bytes, checksum: 6daf4f88308c3c733615f0772d6db594 (MD5) / Made available in DSpace on 2017-05-12T14:19:07Z (GMT). No. of bitstreams: 1 2010 - Henriqueta Talita Guimar?es Barboza.pdf: 10302674 bytes, checksum: 6daf4f88308c3c733615f0772d6db594 (MD5) Previous issue date: 2010-03-04 / Twelve heterocyclic dialkylphosphorylhydrazones compounds were synthesized in this work. Dialkylphosphorylhydrazones were obtained through 3 steps of reaction. The first step consists on the synthesis of different dialkylphosphonates obtained by reaction of triethyl phosphate (PCl3) with 3 mols of the corresponding alcohol. The second step occurs by the reaction with dialkylphosphonates synthesized and hydrazine, producing dialkylphosphorylhydrazines. The third and last step is the condensation reaction of these dialkylphosphorylhydrazines with different heterocycle substituted aromatic aldehydes. The analysis of the 1H NMR spectra allowed to observe the stereoisomers E and Z, with the formation of E diastereisomer preferencially. All the compounds were characterized by 1H, 13C and 31P NMR, IR and mass spectroscopy. Tests in vitro with, Alternaria sp., Colletotrichum sp., Fusarium sp. e Fusarium solani, known as patogenic in papaya (Carica papaya L.) were performed in order to confirm if the compounds showed fungicide activity. The substance 6 B was the one with the best performance in the inhibition of all fungal growths. Finally, tests with acetylcholinesterase enzyme indicated that all substances did not inhibit this enzyme. Figure 2 - General structures of dialkylphosphoryhidrazones synthesized. R ? Ethyl; propyl; isopropyl e isobuthyl. X = O, Y, Z e W = CH; X = S, Y, Z e W = CH; X = NH, Y, Z e W = CH; X = NH, Y= CH, Z=CH e W = N; X = CH, Y= N, Z=CH e W = N; / Neste trabalho foram sintetizadas doze (12) novas dialquilfosforilidrazonas heteroc?clicas. Esses compostos foram obtidos utilizando-se tr?s etapas de rea??o. A primeira etapa consiste na s?ntese de diferentes fosfonatos de dialquila, obtidos por meio da rea??o do tricloreto de f?sforo (PCl3) com tr?s mols do ?lcool correspondente. A segunda etapa ocorre por meio da rea??o dos fosfonatos de dialquila sintetizados com a hidrazina, formando as dialquilfosforilidrazinas. A terceira e ?ltima etapa ? a condensa??o destas dialquilfosforilidrazinas com diferentes alde?dos heteroc?clicos. A an?lise dos espectros de RMN-1H indica a forma??o de diastereois?meros, E e Z, com predomin?ncia do diastereis?meros E. Todos os compostos obtidos foram caracterizados por RMN de H1 e C13 e P31, IV, an?lises de massas. Em seguida foram realizados testes in vitro para verificar se os mesmos possuem atividade fungicida sobre os fungos Alternaria sp., Colletotrichum sp., Fusarium sp. e Fusarium solani, conhecidos por serem pat?genos da cultura de mam?o (Carica papaya L.). O composto 6 B foi o que apresentou o melhor efeito fungicida sobre o crescimento de todos os fungos. Finalmente foram realizados testes com a enzima acetilcolinesterase a fim de observar a toxicidade dos compostos sintetizados frente a esta enzima. Figura 1- Estrututa gen?rica das dialquilfosforilidrazonas heteroc?clicas sintetizadas. R ? Etil; propil; isopropil e isobutil. X = O, Y, Z e W = CH; X = S, Y, Z e W = CH; X = NH, Y, Z e W = CH; X = NH, Y= CH, Z=CH e W = N; X = CH, Y= N, Z=CH e W = N.